OSCR

Cell-type-specific circadian and light-responsive transcriptional dynamics in adult <i>Drosophila</i> neurons.

Overview

Authors: Gillian Berglund1,2, Pranav Ojha1,2, Maria Ivanova1,2, Melina Pérez Torres1,2, Michael Rosbash1,2
  1. HHMI, Brandeis University, Waltham, MA 02454
  2. Department of Biology, Brandeis University, Waltham, MA 02454
Institutions: Brandeis University (United States)
Dates: received 29 May 2026; accepted 6 August 2026; published online 8 September 2026; in print 15 September 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1073/pnas.2619143123 · PMID 42709819 · PMCID PMC13578309 · OpenAlex W7211947821
Open access: hybrid, a free copy (OpenAlex)
Status: data only
Categories: genetics / omics (modality), drosophila (organism), cellular / molecular (subfield)
Methods: Evoked potentials
Keywords: circadian neurons, snRNA-Seq, immediate-early genes
MeSH: Circadian Rhythm*, Drosophila melanogaster*, Neurons*, Transcription, Genetic*, Animals, Drosophila Proteins, Gene Expression Regulation, Light, Transcriptome (* major topic)
Journal subjects: Biological Sciences, Genetics
Topic: Circadian rhythm and melatonin (Endocrine and Autonomic Systems, Neuroscience), according to OpenAlex
Citations: cited by 1 paper (Europe PMC); 54 references in the paper

Abstract

The Drosophila adult central brain contains 240 circadian neurons, of which there are more than 25 different neuron subtypes based on connectomic data. Recent single-cell RNA-seq characterization of these neurons “around the clock” also indicates a similar number of molecular subtypes of circadian neurons, but other conclusions from these transcriptomic studies warranted verifying and extending with other approaches. To address these limitations, we used three complementary approaches: 1) We used a genetic multiplexing strategy to profile the transcriptomes of circadian neurons from multiple time points in a single experiment, reducing confounding technical variation between timepoints; 2) Large numbers of single nuclei were sequenced (snRNA-seq), which was enabled because the method El-INTACT purifies nuclei from frozen heads; 3) We assayed 12 time points under both light–dark and constant darkness conditions. These approaches showed dramatic transcriptional differences between time points in many circadian neuron types and enhanced time-of-day gene expression analysis. The data indicate that most of this regulation is transcriptional and circadian. There were however a small number of light-dependent transcripts, including some that correspond to mammalian immediate-early genes. They probably play a role in the light-regulation of gene expression and behavior in specific neurons, perhaps circadian entrainment or phase-shifting. The results taken together provide a more comprehensive picture of gene expression heterogeneity within adult Drosophila circadian neurons including how intrinsic clock mechanisms and light cues are integrated across circadian neuron subtypes.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

The paper links to its data, not to its authors' code: see the Data section.

The paper's code and data availability statement is in the Data section.

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Data

Datasets cited

Data, Materials, and Software Availability

The snRNA-seq data have been deposited in the Gene Expression Omnibus (GEO) under accession no. GSE325877 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE325877) (54).

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 5 authors, 3 keywords, 9 MeSH terms, 1 funder, 54 references.

Cite

This paper

Berglund, G., Ojha, P., Ivanova, M., Pérez Torres, M., & Rosbash, M. (2026). Cell-type-specific circadian and light-responsive transcriptional dynamics in adult <i>Drosophila</i> neurons. Proceedings of the National Academy of Sciences of the United States of America, 123(37), e2619143123. https://doi.org/10.1073/pnas.2619143123

BibTeX

@article{berglund2026cell,
author = {Berglund, Gillian and Ojha, Pranav and Ivanova, Maria and Pérez Torres, Melina and Rosbash, Michael},
title = {{Cell-type-specific circadian and light-responsive transcriptional dynamics in adult \<i\>Drosophila\</i\> neurons}},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
year = {2026},
month = sep,
volume = {123},
number = {37},
pages = {e2619143123},
publisher = {National Academy of Sciences},
issn = {0027-8424},
doi = {10.1073/pnas.2619143123},
url = {https://doi.org/10.1073/pnas.2619143123},
pmid = {42709819},
pmcid = {PMC13578309}
}

RIS

TY - JOUR
AU - Berglund, Gillian
AU - Ojha, Pranav
AU - Ivanova, Maria
AU - Pérez Torres, Melina
AU - Rosbash, Michael
TI - Cell-type-specific circadian and light-responsive transcriptional dynamics in adult <i>Drosophila</i> neurons
T2 - Proceedings of the National Academy of Sciences of the United States of America
J2 - Proc Natl Acad Sci U S A
PY - 2026
DA - 2026/09/08
VL - 123
IS - 37
SP - e2619143123
SN - 0027-8424
PB - National Academy of Sciences
DO - 10.1073/pnas.2619143123
UR - https://doi.org/10.1073/pnas.2619143123
LA - en
ER -

CSL-JSON

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